18 job matcher din søgning
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within drug development - and are you passionate about the voice of patients and their caregivers?
Lundbeck’s focus is first and foremost on the patients suffering from Alzheimer’s Disease, Parkinson’s Disease, depression and schizophrenia, for whom we develop innovative medical treatments. In the Medical & Regulatory Science business unit, we strive to integrate patient perspectives in our activities.
Your job will be at the center of this, helping us to develop and operationalize patient and caregiver insights linked to the regulatory and medical aspects of our drug development strategies. We would therefore expect you to have a passion for patient focused drug development combined with the skills and educational background to understand and navigate medical and scientific data.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Nonclinical Safety Research in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges across the company. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
We are searching for a graduate, with an interest in nonclinical activities, to support our development projects and marketed products. Your “home base” will be in Department of Bioanalysis, but you will work closely with other departments inside and outside Nonclinical Safety Research.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Clinical Pharmacology in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges cross functionally. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
We are searching for a graduate who can support Quantitative Pharmacology in the daily work and help us in our mission to become a world class pharmacometric service provider for Lundbeck.
We are looking for an experienced academic for a new position in Analytical Development, that will provide scientific leadership and coordination for analytical development activities.
You will be responsible for the analytical development in our global development projects within our highly integrated CMC project organization. You will lead the analytical development for small molecule API’s and IMP for clinical studies, and ensuring sufficient quality of release- and stability analyses, and coordination of project activities across the organization.
You will be an active member of the CMC focus team(s), and your responsibilities include:
- Analytical development, validation, release and stability studies, covering both API and drug product for the given project
- Ensuring flexible planning and coordination of analytical tasks and matching the shifting project demands over time, including scenario planning
Zealand Pharma A/S, Glostrup
Zealand Pharma A/S (Zealand) is looking for an experienced patent attorney to join the IP Department, which presently counts two patent attorneys and one assistant. Key responsibilities will include building up IP strategies, patent application drafting, filing and prosecution together with patent search and analysis.
Zealand has built a large and diversified patent portfolio, and considers protection of inventions in peptide drug discovery and development to be key to our business success.
We offer a combined salary package including pension scheme and health insurance, as well as the option of joining the company lunch program, and use of massage, fitness and social facilities.
Chr. Hansen A/S, Hørsholm
Use your technical Dairy technology expertise in the interaction with global customers.
In Chr. Hansen we are working with Application in the HQ and in our Regional and Local Labs around the world (e.g. Regional lab in Argentina, Local in Brazil). We have well-equipped dairy pilot plants and laboratories and we are always striving to coordinate activities around the world and express everybody’s full potential.
- Develop your dairy application skills within the Fresh Dairy, Cheese and BioProtection segments enabling you to provide top-class technical advice and trouble-shooting to our customers
- Plan, perform and report on trials. Hands-on work in the pilot dairy and laboratories will be part of your assignments
- Drive Application projects within the Dairy segments, securing timely and successful deliverables
Bavarian Nordic A/S, Kvistgård
Do you like to take responsibility and always ensure your process is in compliance and ready for operation? Then you are the one we are looking for right now!
Our production site is under development since we are building a new filling plant with isolator technology and freeze drying. Therefor we are looking for a process specialist who has solid experience within cleanroom facilities, environmental monitoring and cleaning validation.
As Process Specialist your primary responsibility will be implementation and validation of environmental monitoring both in the facility and the processes so that we can obtain the necessary approvals of both equipment and processes. You will be involved in protocol and report writing on qualifications, as well as SOP writing and work within GMP and BSL rules.
ORIGIO a/s, Måløv
Vi søger til snarest mulig tiltrædelse en procesoperatør til vores sterilproduktion i Måløv, som sammen med det øvrige produktionsteam skal deltage og tage ansvar i alle de daglige arbejdsopgaver i produktionen, herunder:
- Aseptisk fremstilling og afvejning af råvarer via vejekontrolssoftware.
- Sterilfiltrering af flydende medier.
- Aseptisk påfyldning af sterile medier på tekniske påfyldningslinjer, kan i enkelte tilfælde udføres manuelt.
- Indslusning af materialer og råvarer til renrum (ISO kl. 5-8).
- Deltagelse i løbende forbedringsprojekter med fokus på robuste løsninger.
- Vask og rengøring af utensilier, udstyr og maskiner samt 0-stilling af lokaler.
- Ad hoc-opgaver i både Produktion og Pakkeri m.m.
Senior Specialist Pharmacovigilance
Zealand Pharma A/S, Glostrup
Are you passionate about making a true difference for patients by using your expertise in our clinical development activities in rare diseases? Are you also thinking of making a career change and being part of a very dynamic, ambitious, professional, yet lean team where you can have influence?
Then you may be our new colleague in Regulatory, Pharmacovigilance and Medical Writing.
Zealand Pharma A/S (Zealand) is looking for a Pharmacovigilance Senior Specialist who will report to the Head of Pharmacovigilance. The Senior Specialist will have as key responsibilities:
- Ongoing safety surveillance
- Signal management
- Aggregated safety reporting
If you are passionate about automation and packaging equipment, have strong IT skills and experience in working with implementation and optimization of manufacturing equipment this job is a great opportunity for you.
As Support and Optimization engineer you will play an important role in our continuous work to improve our processes and equipment with the aim of increasing Overall Equipment Efficiency (OEE). You will be responsible for a portfolio of upgrade and optimization activities across our packaging lines, managing the entire process from registration over prioritization, planning, through execution and final evaluation of the individual projects and tasks.
You will drive the systematic evaluation of proposed improvements by collecting relevant data, performance of structured problem analysis and cost benefit calculations. Also, you will participate in defining and follow-up on the execution of activity plans.
Would you like to take on an influential role as Global Key Account Manager and embark on an incredible and challenging journey? Then this is your opportunity to be part of our highly skilled and ambitious team!
As Key Account Manager, you will be expected to develop close relations and a broad network in the customers headquarter and regional centers and to gain insight in the customers strategic agenda, understanding how this agenda can be furthered by FOSS' solutions.
You will gain insight in the customers installed base and plans for investments in analytical equipment, as well as promote FOSS' portfolio and uncover opportunities not included in the customer’s investment plans.
We are looking for a talented, experienced and action-oriented Head of Global Market Research to lead the Global Market Research team.
Reporting directly to the Head of Global Market Analysis, the Head of Global Market Research leads the global market research team and is accountable for the development and execution of market research and insights generation in close collaboration with affiliates, internal- and external stakeholders.
The Head of Global Market Research is responsible for the daily management, leadership, recruitment, appraising, developing and coaching of the global market research team (two direct reports), creating a high-performing team that generates valuable market research for various processes.
Vivostat A/S, Allerød
Providing professional support to our distributor network is key to this role. The support takes on many forms and shapes, ranging from technical support with our equipment to clinical application questions across a wide range of indications. It also includes on-site application support and training of medical professionals in hospitals (OR’s) together with territory managers from our distributors.
Our new product and application specialist will also be involved in marketing activities, e.g. organizing conference participation/exhibition and the annual distributor seminar. You will report to the Sales and Marketing Manager.
Duties and responsibilities
- Educate and train distributor staff in the proper use of our products
- Train medical professionals in the most appropriate use of our products
- Support our distributors with product and clinical information.
Jobindex A/S recruiting on behalf of Aquaporin in Lyngby
Join the only company that has managed to commercialize water purifying aquaporin-based membranes. By guiding product specification and qualification as a core member of Product Development team, you will be a significant contributor to the expansion of our product lineup in the brackish water purification market using our unique membrane technology.
In other words, you get to develop our water purification technology to meet the needs of our growing customer base. And you do so as part of a great and friendly team where we succeed through collaboration – and in a jovial atmosphere where we celebrate victories big and small. Also, you will be encouraged to innovate ideas and patent them in the pursuit of the next big breakthrough.
Corporate Product Quality Control søger en analysekemiker med lyst til at indgå i et udfordrende og resultatorienteret arbejdsmiljø. Afdelingen beskæftiger p.t. 84 medarbejdere.
Områdets hovedansvarsområde er udførelse af QA/QC-opgaver relateret til Lundbecks produktion, dvs. ansvaret for kvalitetskontrol og frigivelse af aktive stoffer, råvarer, samt de farmaceutiske bulk produkter, hvori disse indgår. Vi arbejder tæt sammen med produktionsafdelingerne i denne proces. Endvidere udfører vi holdbarhedsstudier, udvikling og validering af analysemetoder, overførsel af analytiske metoder til samarbejdspartnere verden over, samt trouble shooting i samarbejde med produktionsafdelingerne og R&D.
Som analysekemiker vil du indgå i en af områdets 4 sektioner. Sektionen er et dynamisk team bestående af 10 laboranter og 8 akademikere, som primært beskæftiger sig med tablet kampagneprodukter samt alle Lundbecks flydende produkter.
Novo Nordisk Foundation Center for Biosustainability (DTU Biosustain) is establishing a scale-up/-down piloting facility to commercialize bio-based products and molecules for a variety of customers and application markets.
The work of the Piloting Facility of the Center aims towards bridging the gap between academic metabolic engineering projects from cell factories and their commercial application.
If you identify yourself with such a mindset, are interested to transition multiple organisms from micro-scale through bench-scale into multi-kilo scale, advance the processes further into commercialization through contract manufacturing, spin-outs, sales and licensing, and have confidence and enthusiasm for the bio-based economy, as we have, you should apply.
Are you passionate about pharmacovigilance and psychiatry? Do you want to be part of a committed medical safety team engaged with the clinical development and life-cycle management of psychiatric medicine? Do you have strong background in pharmacovigilance and as a clinician, preferable in psychiatry? Do you possess the leadership skills to lead a safety team and cross-functional safety committees? If so, you may be our new Senior Safety Physician in Medical Safety Psychiatry.
Reporting to the Director of Medical Safety - Psychiatry, your responsibilities will be to lead safety teams in the Medical Safety - Psychiatry Department. You will be responsible for all aspects of clinical safety & surveillance related to allocated psychiatry projects/products.
We are looking for a highly motivated research assistant to join the discovery of new innovative treatments for brain disorders. The Department of Molecular Screening is responsible for molecular pharmacology and screening support for Lundbeck’s drug discovery projects. Techniques represented in the Department include molecular pharmacology, electrophysiology and various cell-based and biochemical assays to profile small molecules and biologics.
You will be part of a team providing molecular pharmacology and screening support for research projects aiming for new drug candidates for psychiatric and neurological diseases. You will be responsible for planning and executing studies and reporting these to project teams.